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Items: 3

1.
A bone mineralization defect in the Pahenu2 model of classical phenylketonuria involves compromised mesenchymal stem cell differentiation
Steven F. Dobrowolski, Irina L. Tourkova, Lisa J. Robinson, Cassandra Secunda, Kayla Spridik, Harry C. Blair
Mol Genet Metab. Author manuscript; available in PMC 2019 Nov 1.
Published in final edited form as: Mol Genet Metab. 2018 Nov; 125(3): 193–199. Published online 2018 Aug 27. doi: 10.1016/j.ymgme.2018.08.010
PMCID:
PMC6542264
ArticlePDF–623K
2.
Long-term dietary intervention with low Phe and/or a specific nutrient combination improve certain aspects of brain functioning in phenylketonuria (PKU)
Vibeke M. Bruinenberg, Danique van Vliet, Els van der Goot, Danielle S. Counotte, Mirjam Kuhn, Francjan J. van Spronsen, Eddy A. van der Zee
PLoS One. 2019; 14(3): e0213391. Published online 2019 Mar 15. doi: 10.1371/journal.pone.0213391
PMCID:
PMC6420157
ArticlePDF–2.6M
3.
Targeting mGlu5 Metabotropic Glutamate Receptors in the Treatment of Cognitive Dysfunction in a Mouse Model of Phenylketonuria
Francesca Nardecchia, Rosamaria Orlando, Luisa Iacovelli, Marco Colamartino, Elena Fiori, Vincenzo Leuzzi, Sonia Piccinin, Robert Nistico, Stefano Puglisi-Allegra, Luisa Di Menna, Giuseppe Battaglia, Ferdinando Nicoletti, Tiziana Pascucci
Front Neurosci. 2018; 12: 154. Published online 2018 Mar 16. doi: 10.3389/fnins.2018.00154
PMCID:
PMC5864888
ArticlePDF–1.6M

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